A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051484



Internal ID19140703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131850783..131872374hg38UCSC Ensembl
Innerchr9:134726170..134747761hg19UCSC Ensembl
Innerchr9:133715991..133737582hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3821592
hg1921592
hg1821592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695291, nssv3695290
Samples
Known GenesMED27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051484
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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